Papers
RefSeq ID
Protein change
DNA change
Selected Variant
NM_000406.3
p.R262Q
c.785G>A
Surrounding Variants
NM_000406.3
p.R262P
c.785G>C
NM_000406.3
p.R262W
c.784C>T
NM_000406.3
p.R262G
c.784C>G
NM_000406.3
p.R262delFs
c.785delC
NM_000406.3
p.A261V
c.782C>T
NM_000406.3
p.A261G
c.782C>G
NM_000406.3
p.A261E
c.782C>A
NM_000406.3
p.A261S
c.781G>T
NM_000406.3
p.A261P
c.781G>C
NM_000406.3
p.K264*
c.790A>T
NM_000406.3
p.K264Q
c.790A>C
NM_000406.3
p.R260insFs
c.778_779insA